Ingo Kennerknecht

Genotype–phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21

Robert Lyle, Frédérique Béna, Sarantis Gagos et al. · European Journal of Human Genetics · 2008 · 325 citations · Full text

Down Syndrome, Array Cgh, Cytogenetics +6

First report of prevalence of non‐syndromic hereditary prosopagnosia (HPA)

Ingo Kennerknecht, Thomas Grueter, Brigitte Welling et al. · American Journal of Medical Genetics Part A · 2006 · 267 citations

Family Members, Corticobasal Degeneration, Genetic Epidemiology +18

Hereditary Prosopagnosia: the First Case Series

M. Grueter, Thomas Grueter, Vaughan Bell et al. · Cortex · 2007 · 143 citations

First Case Series, Anatomy, Developmental Anomaly

MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta

Uschi Lindert, Wayne A. Cabral, Surasawadee Ausavarat et al. · Nature Communications · 2016 · 141 citations · Full text

Prevalence of hereditary prosopagnosia (HPA) in Hong Kong Chinese population

Ingo Kennerknecht, Nga Yee Ho, Virginia Wong · American Journal of Medical Genetics Part A · 2008 · 113 citations

Hereditary Prosopagnosia, Developmental Anomaly, Psychiatry +15